Details for New Drug Application (NDA): 008453
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NDA 008453 describes ANECTINE, which is a drug marketed by Sandoz and is included in one NDA. It is available from three suppliers. Additional details are available on the ANECTINE profile page.
The generic ingredient in ANECTINE is succinylcholine chloride. There are six drug master file entries for this compound. Twenty-nine suppliers are listed for this compound. Additional details are available on the succinylcholine chloride profile page.
The generic ingredient in ANECTINE is succinylcholine chloride. There are six drug master file entries for this compound. Twenty-nine suppliers are listed for this compound. Additional details are available on the succinylcholine chloride profile page.
Summary for 008453
| Tradename: | ANECTINE |
| Applicant: | Sandoz |
| Ingredient: | succinylcholine chloride |
| Patents: | 0 |
Pharmacology for NDA: 008453
| Physiological Effect | Neuromuscular Depolarizing Blockade |
Medical Subject Heading (MeSH) Categories for 008453
Suppliers and Packaging for NDA: 008453
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| ANECTINE | succinylcholine chloride | INJECTABLE;INJECTION | 008453 | NDA | Sandoz Inc | 0781-3411 | 0781-3411-95 | 10 VIAL, MULTI-DOSE in 1 CARTON (0781-3411-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-3411-70) |
| ANECTINE | succinylcholine chloride | INJECTABLE;INJECTION | 008453 | NDA | Sandoz Inc | 0781-9053 | 0781-9053-95 | 10 VIAL, MULTI-DOSE in 1 CARTON (0781-9053-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-9053-70) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 500MG/VIAL | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 20MG/ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | AP | RLD: | Yes | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 50MG/ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
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